20068-10-4

Basic information

• Product Name: 3-Butenenitrile, 4-phenyl-, (E)-
• Synonyms: (E)-4-phenylbut-3-enenitrile;4-phenyl-but-3-enenitrile;(E)-4-Phenyl-but-3-enenitrile;1-cyano-3-phenyl-2-propene;4-phenylbut-3-enenitrile
• CAS NO: 20068-10-4
• Molecular Formula: C10H9N
• Molecular Weight: 143.188
• Mol File: 20068-10-4.mol
• Article Data: 27

Chemical Properties

• Melting Point: 59-60 °C
• Boiling Point: 286.9±19.0 °C(Predicted)
• Density: 1.020±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 3-Butenenitrile, 4-phenyl-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Butenenitrile, 4-phenyl-, (E)-(20068-10-4)
• EPA Substance Registry System: 3-Butenenitrile, 4-phenyl-, (E)-(20068-10-4)

Safety Data

• Hazardous Substances Data: 20068-10-4(Hazardous Substances Data)

Upstream product

• 43219-51-8 (E)-(3-isocyanoprop-1-en-1-yl)benzene 
• 143-33-9 sodium cyanide 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 151-50-8 potassium cyanide 
• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 201230-82-2 carbon monoxide 
• 122-78-1 phenylacetaldehyde 
• 372-09-8 cyanoacetic acid 
• 10442-39-4 tetra-n-butylammonium cyanide 
• 91970-13-7 1-((E)-3-(methoxymethoxy)prop-1-enyl)benzene 
• 6783-05-7 trans-2-phenylvinylboronic acid 
• 6011-14-9 2-aminoacetonitrile hydrochloride 
• 106625-69-8 ethyl (E)-3-phenyl-2-propenyl carbonate 
• 28321-12-2 (E)-(4,4-difluorobuta-1,3-diene-1-yl)benzene 

Downstream Products

• 40595-34-4 (E)-trimethyl(3-phenylallyl)silane 
• 2046-18-6 4-phenylbutyronitrile 
• 2243-53-0 trans-styrylacetic acid 
• 1205-84-1 ethyl (E)-4-phenylbut-3-enoate 
• 220429-71-0 (E)-5-(2-phenylethenyl)-1H-tetrazole 
• 20068-09-1 (Z)-4-phenylbut-3-enenitrile 
• 139688-52-1 Trifluoro-methanesulfonate1,4-dimethyl-5-((E)-3-phenyl-allyl)-4H-tetrazol-1-ium; 
• 85234-94-2 1-cyano-3-methoxy-3-phenyl-1(E)-propene 
• 139688-84-9 Trifluoro-methanesulfonatemethyl-((E)-4-phenyl-but-3-enylidyne)-ammonium; 
• 83144-20-1 (E)-4-hydroxy-4-phenyl-2-butenenitrile 
• 110036-07-2 ((E)-4-Phenyl-2-triisopropylsilanyl-buta-1,3-dienylidene)-triisopropylsilanyl-amine 
• 20067-97-4 cis-4-phenyl-2-butenenitrile 
• 20067-98-5 trans-4-phenyl-2-butenenitrile 

Relevant articles and documents

Rapid and Simple Access to α-(Hetero)arylacetonitriles from Gem-Difluoroalkenes

A scalable cyanation of gem-difluoroalkenes to (hetero)arylacetonitrile derivatives was developed. This strategy features mild reaction conditions, excellent yields, wide substrate scope, and broad functional group tolerance. Significantly, in this reacti

Photo-Promoted Decarboxylative Alkylation of α, β-Unsaturated Carboxylic Acids with ICH2CN for the Synthesis of β, γ-Unsaturated Nitriles

An efficient, catalyst/photocatalyst-free, and cost-effective methodology for the decarboxylative alkylation of α,β-unsaturated carboxylic acids to synthesize β,γ-unsaturated nitriles has been developed. The reaction proceeded in an environmentally benign atmosphere of blue light-emitting diode irradiation with K2CO3 and water at room temperature. The methodology worked for a wide range of substrates (22 examples) with up to 83% yield. The protocol is also compatible for gram-scale synthesis.

Synthesis method of (E)-4-aryl-3-butenonitrile compound

The invention belongs to the technical field of organic synthesis chemistry, and discloses a synthesis method of a (E)-4-aryl-3-butenonitrile compound. According to the method, under catalysis of copper iodide, a target compound is synthesized in one step